首页> 外国专利> Process for the prepn. of cell-free penicillin-acylase by fermenting a strain of E. coli which produces this enzyme. The intracellular enzyme is separated form

Process for the prepn. of cell-free penicillin-acylase by fermenting a strain of E. coli which produces this enzyme. The intracellular enzyme is separated form

机译:准备过程。通过发酵产生这种酶的大肠杆菌菌株来制备无细胞的青霉素酰基转移酶。细胞内酶分离形式

摘要

Prepn. of cell-free penicillin-acylase by fermenting a strain of E. coli which produces this enzyme. The intracellular enzyme is separated from the culture liquid at controlled temps. between 0-50 deg.C by fast removal of the cell material through a slot or opening at a pressure of at least 500 psi but below the pressure which would badly tear the cells. The removed cell material is then stirred in water for 0.1-5 hrs. at 10-50 deg.C to dissolve the enzyme; this is extracted from the inactive cell material in aqs. soln. The cell-free enzymes are used for the prodn. of 6-APA and are esp. suitable for direct removal of side-chains of natural penicillins, esp. the side-chains of benzyl penicillin. The enzymes may be used as starting materials for chemical modification of the enzyme, giving products with higher activity and/or wider technical application.
机译:准备通过发酵产生这种酶的大肠杆菌菌株来制备无细胞的青霉素酰基转移酶。在控制的温度下将细胞内酶与培养液分离。通过在至少500psi但低于会严重撕裂细胞的压力下通过狭缝或开口快速除去细胞材料,可在0-50℃之间进行加热。然后将除去的细胞材料在水中搅拌0.1-5小时。在10-50℃溶解酶;这是从无源细胞材料中提取的。 soln。无细胞酶用于产品。的6-APA,尤其是适用于直接去除天然青霉素的侧链,尤其是。苄青霉素的侧链。所述酶可以用作酶的化学修饰的起始材料,从而提供具有更高活性和/或更广泛的技术应用的产物。

著录项

  • 公开/公告号FR2001977B1

    专利类型

  • 公开/公告日1974-08-30

    原文格式PDF

  • 申请/专利权人 ASTRASW;

    申请/专利号FR19690003732

  • 发明设计人

    申请日1969-02-14

  • 分类号A61K21/00;C07D99/00;C12D13/00;

  • 国家 FR

  • 入库时间 2022-08-23 05:17:34

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